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4-<(7-chloro-4-quinolinyl)amino>-2-<(4-methyl-1-piperazinyl)methyl>phenol 1-oxide is a complex organic compound with a molecular formula of C24H24ClN3O2. This chemical is characterized by a phenol core, which is substituted at the 4-position with an amino group that is connected to a 7-chloro-4-quinolinyl moiety. Additionally, the 2-position of the phenol ring is substituted with a methyl group that is part of a 4-methyl-1-piperazinyl group. The 1-oxide designation indicates that one of the oxygen atoms in the molecule is part of an oxide group. 4-<(7-chloro-4-quinolinyl)amino>-2-<(4-methyl-1-piperazinyl)methyl>phenol 1-oxide is known for its potential applications in the pharmaceutical industry, particularly as an intermediate in the synthesis of certain drugs. Its structure and properties make it a candidate for further research and development in medicinal chemistry.

1055-77-2

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1055-77-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1055-77-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,5 and 5 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1055-77:
(6*1)+(5*0)+(4*5)+(3*5)+(2*7)+(1*7)=62
62 % 10 = 2
So 1055-77-2 is a valid CAS Registry Number.

1055-77-2Downstream Products

1055-77-2Relevant academic research and scientific papers

Anticholinesterase activity of 4-aminoquinolines related to amodiaquine and their respective N-oxides

Go,Ngiam,Lim

, p. 81 - 85 (2007/10/02)

The inhibitory activities of a series of substituted 4-aminoquinolines related to the antimalarial agent amodiaquine and their respective N-oxides toward acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) have been determined and discussed in terms of their proposed mode of interaction with the enzyme surface. A marked difference was noted in the AChE and BChE inhibitory potencies of these compounds. The strong anti-AChE activity of amodiaquine has been explained by a specific two-point interaction with the anionic site and acidic group of AChE. However, such an interaction appears to be absent in the case of the amodiaquine inhibition of BChE, suggesting differences in the ability of the enzymes to accommodate similar inhibitory molecules.

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